Bauhinol E

Details

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Internal ID 109c0105-5fc2-4151-81f6-0abb14e29129
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 5-[2-(2-hydroxyphenyl)ethyl]-3-methoxy-2-methylphenol
SMILES (Canonical) CC1=C(C=C(C=C1OC)CCC2=CC=CC=C2O)O
SMILES (Isomeric) CC1=C(C=C(C=C1OC)CCC2=CC=CC=C2O)O
InChI InChI=1S/C16H18O3/c1-11-15(18)9-12(10-16(11)19-2)7-8-13-5-3-4-6-14(13)17/h3-6,9-10,17-18H,7-8H2,1-2H3
InChI Key JMBBQCITZQVIQJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H18O3
Molecular Weight 258.31 g/mol
Exact Mass 258.125594432 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL390766

2D Structure

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2D Structure of Bauhinol E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.8376 83.76%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.9462 94.62%
OATP2B1 inhibitior - 0.8456 84.56%
OATP1B1 inhibitior + 0.9137 91.37%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7012 70.12%
P-glycoprotein inhibitior - 0.7573 75.73%
P-glycoprotein substrate - 0.7457 74.57%
CYP3A4 substrate + 0.5219 52.19%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate + 0.4683 46.83%
CYP3A4 inhibition - 0.8659 86.59%
CYP2C9 inhibition + 0.6236 62.36%
CYP2C19 inhibition + 0.9163 91.63%
CYP2D6 inhibition - 0.7877 78.77%
CYP1A2 inhibition + 0.8781 87.81%
CYP2C8 inhibition + 0.7485 74.85%
CYP inhibitory promiscuity + 0.7524 75.24%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6954 69.54%
Carcinogenicity (trinary) Non-required 0.6321 63.21%
Eye corrosion - 0.9392 93.92%
Eye irritation + 0.5450 54.50%
Skin irritation - 0.7232 72.32%
Skin corrosion - 0.8084 80.84%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7444 74.44%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5844 58.44%
skin sensitisation - 0.7987 79.87%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7450 74.50%
Acute Oral Toxicity (c) III 0.6663 66.63%
Estrogen receptor binding + 0.5588 55.88%
Androgen receptor binding + 0.7088 70.88%
Thyroid receptor binding + 0.7335 73.35%
Glucocorticoid receptor binding - 0.5171 51.71%
Aromatase binding - 0.5708 57.08%
PPAR gamma + 0.6464 64.64%
Honey bee toxicity - 0.8774 87.74%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9314 93.14%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.16% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.03% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.33% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.51% 95.56%
CHEMBL2535 P11166 Glucose transporter 89.48% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.15% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 86.13% 90.20%
CHEMBL4208 P20618 Proteasome component C5 85.78% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.71% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.39% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.65% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.96% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.10% 99.15%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.42% 89.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.06% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Alnus cordata
Aloe deltoideodonta
Bauhinia purpurea
Crinum latifolium
Hemionitis aschenborniana
Leitneria floridana
Thermopsis mollis

Cross-Links

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PubChem 16680048
NPASS NPC184302
LOTUS LTS0174061
wikiData Q105131221